rs104894063, CHRNA2

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Epilepsy, Nocturnal Frontal Lobe, Type 4
11 0.882 0.120 8 27463607 missense variant A/T snv 0.800 1.000 1 2006 2006
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
8 0.882 0.120 8 27463607 missense variant A/T snv 0.700 0
Nocturnal epilepsy
CUI: C0393719
Disease: Nocturnal epilepsy
2 0.882 0.120 8 27463607 missense variant A/T snv 0.010 1.000 1 2009 2009